Product Recalls in New Jersey

Product recalls affecting New Jersey — including food, drugs, consumer products, medical devices, and vehicles distributed to New Jersey. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,827 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,827 in last 12 months

Showing 63416360 of 29,496 recalls

Medical DeviceMay 22, 2023· Universal Meditech Inc.

Recalled Item: DiagnosUS hCG Pregnancy Serum/Urine Test Cassette Format Recalled by...

The Issue: Universal Meditech Inc. was violatively distributing PrestiBio" Breastmilk...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2023· Universal Meditech Inc.

Recalled Item: HealthyWiser UriTest" UTI Test Strips Recalled by Universal Meditech Inc....

The Issue: Universal Meditech Inc. was violatively distributing PrestiBio" Breastmilk...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2023· Universal Meditech Inc.

Recalled Item: DiagnosUS hCG Pregnancy Urine Test Strip Format Recalled by Universal...

The Issue: Universal Meditech Inc. was violatively distributing PrestiBio" Breastmilk...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2023· Universal Meditech Inc.

Recalled Item: HealthyWiser pH-Aware pH 4.5 - 9.0 pH Test Strips 120 STRIP Recalled by...

The Issue: Universal Meditech Inc. was violatively distributing PrestiBio" Breastmilk...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2023· Universal Meditech Inc.

Recalled Item: DiagnosUS Ovulation Predictor Midstream Recalled by Universal Meditech Inc....

The Issue: Universal Meditech Inc. was violatively distributing PrestiBio" Breastmilk...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2023· Universal Meditech Inc.

Recalled Item: Lem Fertility LH Ovulation Test (Strip) Recalled by Universal Meditech Inc....

The Issue: Universal Meditech Inc. was violatively distributing PrestiBio" Breastmilk...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2023· Universal Meditech Inc.

Recalled Item: One Step Ovulation Test Recalled by Universal Meditech Inc. Due to Universal...

The Issue: Universal Meditech Inc. was violatively distributing PrestiBio" Breastmilk...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2023· Universal Meditech Inc.

Recalled Item: HealthyWiser KetoFast" Ketone Test Strips 150 test strips Recalled by...

The Issue: Universal Meditech Inc. was violatively distributing PrestiBio" Breastmilk...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2023· Universal Meditech Inc.

Recalled Item: To Life hCG Pregnancy Urine Test Strips Format No: 100-10 Recalled by...

The Issue: Universal Meditech Inc. was violatively distributing PrestiBio" Breastmilk...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2023· Universal Meditech Inc.

Recalled Item: PrestiBio BREAST MILK ALCOHOL TEST STRIP 25 TESTS Recalled by Universal...

The Issue: Universal Meditech Inc. was violatively distributing PrestiBio" Breastmilk...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2023· Universal Meditech Inc.

Recalled Item: Am I Pregnant? One Step HCG Pregnancy Test Recalled by Universal Meditech...

The Issue: Universal Meditech Inc. was violatively distributing PrestiBio" Breastmilk...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2023· Universal Meditech Inc.

Recalled Item: PrestiBio Pregnancy Strips 25 HCG Test Strips Recalled by Universal Meditech...

The Issue: Universal Meditech Inc. was violatively distributing PrestiBio" Breastmilk...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2023· CareFusion 303, Inc.

Recalled Item: BD Pyxis CII Safe Recalled by CareFusion 303, Inc. Due to Automated...

The Issue: Automated dispensing cabinet devices plugged into any multi-socket outlet...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2023· Wilson-Cook Medical Inc.

Recalled Item: Hemospray Endoscopic Hemostat: Part Numbers: a) HEMO-10 Recalled by...

The Issue: There are potential risks of the Hemospray powder adhering to the distal end...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2023· Wilson-Cook Medical Inc.

Recalled Item: Hemospray Endoscopic Hemostat: Part Numbers: a) HEMO-7 Recalled by...

The Issue: There are potential risks of the Hemospray powder adhering to the distal end...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2023· Olympus Corporation of the Americas

Recalled Item: UroPass Ureteral Access Sheaths Recalled by Olympus Corporation of the...

The Issue: Dilator tips may break in the package and in patients during surgical...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2023· Ascensia Diabetes Care US, Inc.

Recalled Item: Contour¿ next GEN Blood Glucose Monitoring System Recalled by Ascensia...

The Issue: Ascensia Diabetes Care has determined through customer complaints that 580...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2023· Baxter Healthcare Corporation

Recalled Item: NaviCare Patient Safety V3.9.200 to 3.9.600 Recalled by Baxter Healthcare...

The Issue: Baxter identified a potential risk where the "safety" monitoring and "bed...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2023· Baxter Healthcare Corporation

Recalled Item: Voalte Patient Safety Recalled by Baxter Healthcare Corporation Due to...

The Issue: Baxter identified a potential risk where the "safety" monitoring and "bed...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2023· ARROW INTERNATIONAL Inc.

Recalled Item: ARROW Endurance Extended Dwell Peripheral Catheter System Recalled by ARROW...

The Issue: Potential for catheter separation or leakage

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing